An Alternative Synthesis of
2-Alkylidene-3,4-dihydro-2H-1,4-benzoxazines by
Intramolecular Gold-Catalyzed Hydroalkoxylation of 2-(Prop-2-yn-1-ylamino)phenols

Angelo M. Manzo; Alcide Perboni; Gianluigi Broggini; Micol Rigamonti

doi:10.1055/s-0030-1258346

PAPER

An Alternative Synthesis of 2-Alkylidene-3,4-dihydro-2H-1,4-benzoxazines by Intramolecular Gold-Catalyzed Hydroalkoxylation of 2-(Prop-2-yn-1-ylamino)phenols

Angelo M. Manzo*^a, Alcide Perboni^a, Gianluigi Broggini*^b, Micol Rigamonti^b
^a Chemical Development, GlaxoSmithKline Medicine Research Center, via Fleming 4, 37135 Verona, Italy
Fax: +39(045)8218117; e-Mail: angelomaria.manzo@tin.it;
^b Dipartimento di Scienze Chimiche e Ambientali, Università degli Studi dell’Insubria, via Valleggio 11, 22100 Como, Italy
Fax: +39(031)2386449; e-Mail: gianluigi.broggini@uninsubria.it;

Abstract

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Abstract

An efficient gold-catalyzed procedure to synthesize 2-alkylidene-3,4-dihydro-2H-1,4-benzoxazines has been developed starting from 2-alkynyl-substituted phenols. This is an intramolecular hydroalkoxylation reaction on alkynes tethered to a phenol moiety that represents a valuable alternative to the already reported transition-metal-catalyzed procedures.

Key words

transition metals - heterocycles - alkynes - phenols - fused-ring systems

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Referenzen

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